Tomlinson IP - Search Results

1

Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency.

Alam NA, Rowan AJ, Wortham NC, Pollard PJ, Mitchell M, Tyrer JP, Barclay E, Calonje E, Manek S, Adams SJ, Bowers PW, Burrows NP, Charles-Holmes R, Cook LJ, Daly BM, Ford GP, Fuller LC, Hadfield-Jones SE, Hardwick N, Highet AS, Keefe M, MacDonald-Hull SP, Potts ED, Crone M, Wilkinson S, Camacho-Martinez F, Jablonska S, Ratnavel R, MacDonald A, Mann RJ, Grice K, Guillet G, Lewis-Jones MS, McGrath H, Seukeran DC, Morrison PJ, Fleming S, Rahman S, Kelsell D, Leigh I, Olpin S, Tomlinson IP. Alam NA, et al. Among authors: tomlinson ip. Hum Mol Genet. 2003 Jun 1;12(11):1241-52. doi: 10.1093/hmg/ddg148. Hum Mol Genet. 2003. PMID: 12761039

2

Variants at the secretory phospholipase A2 (PLA2G2A) locus: analysis of associations with familial adenomatous polyposis and sporadic colorectal tumours.

Tomlinson IP, Beck NE, Neale K, Bodmer WF. Tomlinson IP, et al. Ann Hum Genet. 1996 Sep;60(5):369-76. doi: 10.1111/j.1469-1809.1996.tb00434.x. Ann Hum Genet. 1996. PMID: 8912789

3

Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancer.

Tomlinson IP, Beck NE, Homfray T, Harocopos CJ, Bodmer WF. Tomlinson IP, et al. J Med Genet. 1997 Jan;34(1):39-42. doi: 10.1136/jmg.34.1.39. J Med Genet. 1997. PMID: 9032648 Free PMC article.

4

Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteria.

Beck NE, Tomlinson IP, Homfray T, Frayling I, Hodgson SV, Harocopos C, Bodmer WF. Beck NE, et al. Among authors: tomlinson ip. Hum Genet. 1997 Feb;99(2):219-24. doi: 10.1007/s004390050343. Hum Genet. 1997. PMID: 9048925

5

Beta-catenin mutations in cell lines established from human colorectal cancers.

Ilyas M, Tomlinson IP, Rowan A, Pignatelli M, Bodmer WF. Ilyas M, et al. Among authors: tomlinson ip. Proc Natl Acad Sci U S A. 1997 Sep 16;94(19):10330-4. doi: 10.1073/pnas.94.19.10330. Proc Natl Acad Sci U S A. 1997. PMID: 9294210 Free PMC article.

6

Defects in mismatch repair occur after APC mutations in the pathogenesis of sporadic colorectal tumours.

Homfray TF, Cottrell SE, Ilyas M, Rowan A, Talbot IC, Bodmer WF, Tomlinson IP. Homfray TF, et al. Among authors: tomlinson ip. Hum Mutat. 1998;11(2):114-20. doi: 10.1002/(SICI)1098-1004(1998)11:2<114::AID-HUMU3>3.0.CO;2-J. Hum Mutat. 1998. PMID: 9482574

7

Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases.

Houlston R, Bevan S, Williams A, Young J, Dunlop M, Rozen P, Eng C, Markie D, Woodford-Richens K, Rodriguez-Bigas MA, Leggett B, Neale K, Phillips R, Sheridan E, Hodgson S, Iwama T, Eccles D, Bodmer W, Tomlinson I. Houlston R, et al. Hum Mol Genet. 1998 Nov;7(12):1907-12. doi: 10.1093/hmg/7.12.1907. Hum Mol Genet. 1998. PMID: 9811934

8

Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.

Ylikorkala A, Avizienyte E, Tomlinson IP, Tiainen M, Roth S, Loukola A, Hemminki A, Johansson M, Sistonen P, Markie D, Neale K, Phillips R, Zauber P, Twama T, Sampson J, Järvinen H, Mäkelä TP, Aaltonen LA. Ylikorkala A, et al. Among authors: tomlinson ip. Hum Mol Genet. 1999 Jan;8(1):45-51. doi: 10.1093/hmg/8.1.45. Hum Mol Genet. 1999. PMID: 9887330

9

Genetic aberrations in glioblastoma multiforme: translocation of chromosome 10 in an O-2A-like cell line.

Mao X, Jones TA, Tomlinson I, Rowan AJ, Fedorova LI, Zelenin AV, Mao JI, Gutowski NJ, Noble M, Sheer D. Mao X, et al. Br J Cancer. 1999 Feb;79(5-6):724-31. doi: 10.1038/sj.bjc.6690116. Br J Cancer. 1999. PMID: 10070860 Free PMC article.

10

Somatic mutations in the Peutz-Jeghers (LKB1/STKII) gene in sporadic malignant melanomas.

Rowan A, Bataille V, MacKie R, Healy E, Bicknell D, Bodmer W, Tomlinson I. Rowan A, et al. J Invest Dermatol. 1999 Apr;112(4):509-11. doi: 10.1046/j.1523-1747.1999.00551.x. J Invest Dermatol. 1999. PMID: 10201537 Free article.

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